FDA Adverse Event Malfunction Summary report: N

PIN REV DOME DRILL 25MM

MDR report key: 3914826 · Received July 4, 2014

Report

Report Number
1818910-2014-22709
Event Type
Malfunction
Date Received
July 4, 2014
Date of Event
June 19, 2014
Report Date
June 19, 2014
Manufacturer
DEPUY ORTHOPAEDICS, INC.1818910
Product Code
LXH
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

Additional Manufacturer Narrative · 1

THE DEVICE ASSOCIATED WITH THIS REPORT WAS NOT RETURNED. A COMPLAINT DATABASE SEARCH HAS IDENTIFIED A TREND FOR THIS FAILURE WITHIN THE 2274 QUICKSET DRILL FAMILY. PREVIOUS INVESTIGATIONS HAVE DETERMINED THAT USE ERROR IS THE LIKELY ROOT CAUSE. AS A RESULT OF TRENDING HEALTH HAZARD EVALUATION, DVA-106292-HHE WAS CONDUCTED. THE INVESTIGATION DID NOT ESTABLISH THE NEED FOR CORRECTIVE ACTION. NO EVIDENCE WAS FOUND OF PRODUCT OR DESIGN ERROR AS A CONTRIBUTING FACTOR. SUBSEQUENT COMPLAINTS WILL BE MONITORED UNDER SEP 419 POST MARKET SURVEILLANCE. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY.

Description of Event or Problem · 1

PROCEDURE: TOTAL HIP JOINT REPLACEMENT. DRILL BIT SNAPPED IN THE PELVIS AND IS NOW RETAINED IN THE PATIENT'S BONE. SURGEON X-RAYED PATIENT ON TABLE. HE PALPATED THE POSTERIOR COLUMN AND DEEMED THAT IT WOULD OK FOR THE FRAGMENT TO BE LEFT IN SITU AND NOT RETRIEVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
392882 PIN REV DOME DRILL 25MM HIP INSTRUMENT/TRIAL LXH DEPUY ORTHOPAEDICS, INC.1818910 PG229708

Patients

Seq Age Sex Outcome Treatment
1